Detecting large copy number variants using exome genotyping arrays in a large Swedish schizophrenia sample - Szatkiewicz, J P; Neale, B M; O'Dushlaine, C; Fromer, M; Goldstein, J I; Moran, J L; Chambert, K; Kähler, A; Magnusson, P K E; Hultman, C M; Sklar, P; Purcell, S; et al. (Molecular psychiatry, 2013)
Keywords: 631/208/457/649/2157; 692/699/476/1799; Adult and adolescent clinical studies; Amino acid sequence; Arrays; Autism; Behavioral Sciences; Biological and medical sciences; Biological Psychology; Case-Control Studies; Child development; Chromosomes, Human, Pair 16 - genetics; Chromosomes, Human, Pair 22 - genetics; Copy number; Diagnosis; DNA Copy Number Variations - genetics; Exome - genetics; Gene Deletion; Gene Duplication - genetics; Genetic aspects; Genetics; Genome-wide association studies; Genome-Wide Association Study; Genomes; Genomic structural variations; Genotype; Genotyping; Humans; Hybridization; immediate-communication; Medical sciences; Medicine; Medicine & Public Health; Mental disorders; Neurosciences; Pharmacotherapy; Psychiatry; Psychology. Psychoanalysis. Psychiatry; Psychopathology. Psychiatry; Psychoses; Quality control; Schizophrenia; Schizophrenia - genetics; Sensitivity and Specificity; Sweden; Sweden; United States; United States--US; structural variation; schizophrenia; copy number variation; exome array; Illumina; genotyping; Psychosis; Copy number; Schizophrenia; Genetics; Genetic determinism; Polymorphism